Process to obtain dimers, trimers and up to polymers from pyridinmethanol derivatives compounds

ABSTRACT

The process of the current invention, named Percino-Chapela, has as one of its main novelty features that starting from pyridinmethanol derivatives, a dimerization or polymerization reaction of pyridinic alcohols is carried out in order to produce novel products, the process of the current invention has the following aspects that characterize it: it is carried out in the absence or presence of some solvent, during the process of the current invention, temperature may be or may be not used as catalyst, in the process of the current invention the reaction may be or may not be catalyzed by the presence of a catalyst (acid or base), the resultant products can be produced and separated in an easy way, in the process of the current invention starting from pyridinic alcohols the resultant ethenediols can be produced by a single step reaction, the pyridinmethanol derivatives used as starting compounds, do not oxidize as easily and their handling is easier than that of other compounds previously used that oxidize easily, the products produced with etheneidol parts can be used as antioxidants due to their capacity to act as free radicals scavengers.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit of Mexican Patent Application No. MX/a/2007/009292, filed Aug. 1, 2007, the disclosure of which is hereby incorporated by reference in its entirety.

FIELD OF THE INVENTION

The current invention is referred to the field of certain ethenediol products, as well as to the process to obtain them from pyridine derivatives compounds, it was possible to obtain these products as dimers, trimers up to polymers, which show characteristics as antioxidants due to their ability to inhibit free radicals.

BACKGROUND OF THE INVENTION

Benzoin type condensation is of interest, among other aspects, to: 1) in biochemistry as a model to form carbon-carbon bonds, 2) it is the classical example of specific catalysis, 3) the benzoin condensation shown in reaction 1 below is of organic chemistry relevance for it represents one of the first organic reactions whose mechanism was proposed by Arthur Lapworth. The mechanism is shown in scheme 1. The first step of the reaction is the nucleuphylic attack of the CN⁻ ion to the C═O of the benzaldehyde to form a cyanohydrin, subsequently the cyanohydrin attacks, in a nucleophilic manner, another benzaldehyde molecule to form the corresponding benzoin.

In the above reaction benzaldehyde is used as the starting chemical, while the dimerization of 2-pyridincarboxaldehyde in the presence of KCN produces very stable ethenediols, (C. A. Buehler, Chem. Rev. 1964, 64, 7). From the dimerization of 2-pyridincarboxaldehyde the product 1,2-di(2-pyridyl)ethene-1,2-diol results, this reaction was mistakenly referred to as the pyridoin condensation in resemblance to the benzoin reaction type shown below as Reaction 2. 1,2-Di(2-pyridyl)ethene-1,2-diol produces orange crystals when equal volumes of 2-pyridincarboxaldehyde and glacial acetic acid or KCN are stirred together for several hours.

The benzoin compound has the —COCHOH— group while the ethenediol compounds have the —(HO)C═C(OH)— group.

Polymers with —(HO)C═C(OH)— parts have been prepared by polycondensation of pyridazine-2,3-dialdehyde, pyrazine-2,5-dialdehyde or from pyrimidine-4,6-dialdehyde catalyzed with KCN; the product obtained from these reactions is poly[di-1,2-(diazinilidene)ethene-1,2-diol], as shown in Reaction 3 below, (H. R. Wiley, U.S. Pat. No. 4,260,757).

The drawbacks of the reported procedure to obtain ethenediols are that they are obtained from aromatic aldehydes which, as is well known in organic chemistry, are easily oxidized and therefore have to be previously subjected to purification procedures such as distillation so that they could be used for these type of reactions. The formation of the polymers shown in reaction 3 is from aromatic dialdehydes which are compounds sensitive to air because they are easily oxidized and difficult to obtain for the series of steps involved in the process, furthermore in some cases they are expensive ought to be made in situ to avoid oxidation prior to dimerization. Also, the catalyst (KCN) and solvents must be removed after each reaction to obtain pure products.

From the reaction at high temperature between 2-pyridinecarboxaldehyde and 2-pyridinemethanol, without catalyst and solvent, the product is 2-hydroxy-1,2-(2-pyridyl)-1-ethanone(2), which is deemed to be unstable in solution. Subsequently, compound (2) treated with solvents such as cyclohexane or ethyl acetate produces 1,2-di(pyridin-2-il)etheno-1,2-diol(1) or 1,2-di(pyridin-2-yl)ethane-1,2-dione(3) (2,2′-pyridyl) M. J. Percino, V. M. Chapela, S. Romero, C. Rodriguez-Barbarin, F. J. Melendez-Bustamante Journal of Chemical Crystallography, vol 36(5), 303, (2006) as shown in Reaction 4 that follows.

In addition, in the reaction between 2-pyridinecarboxaldehyde with (6-methylpyridin-2-yl)methanol shown below as reaction 5, the main products obtained are keto-enol compounds: 2-hydroxy-1,2-bis(6-methyl-2-pyridyl)-1-ethanone and 2-hydroxy-1-(6-methyl-2-pyridyl)-2-(2-pyridyl)-1-ethanone. Subsequent treatment with solvent produces 1,2-bis(6-methylpyridin-2-yl)ethane-1,2-dione and 1-(pyridin-2-yl)-2-(6-methylpyridin-2-yl)ethane-1,2-dione and in a much lesser quantity 1,2-bis(6-methylpyridin-2-yl)ethene-1,2-diol (M. J. Percino, V. M. Chapela, O. Urzua, H. Toribio, C. Rodriguez-Barbarin Journal of Chemical Research, (2007), 187).

Reactions identified as 4 and 5, show several disadvantages due to the fact that from the reactions between aromatic aldehydes in the presence of different pyridinemethanol derivatives are produced products such as compound (2) reaction 4, and that by changing the solvent the expected corresponding low molecular weight ethenediols and α-diketones(3) are produced, aside other compounds that are also produced in some instances, this is, there is a mixture of products.

The process of the current invention, named Percino-Chapela has as one of its main novel features that starting from pyridinemethanol derivatives, the dimerization or coupling of pyridinic alcohols reaction is carried out avoiding oxidation as is the case when the starting materials are the corresponding aldehydes. It is a one step process to obtain compounds having the ethenediol group —(HO)—C═C—(OH). The products are orange or brown powders which may indicate a high electronic conjugation in their structure and are soluble in cyclohexane, methanol and DMSO.

The process of the current invention has as characteristic features the following: a) it is carried out in the absence or presence of some solvent, b) in the process of the current invention, the temperature may or may not be used as catalyst, c) in the process of the current invention the reaction may or may not be catalyzed by the presence of a catalyst (acid or base), d) the products may be obtained and separated in an easy way by precipitation, e) in the process of the current invention starting from pyridinic alcohols, ethenediols may be produced, in a single step reaction, f) pyridinemethanol derivatives used as starting chemicals do not oxidize as easily, their handling is not complex and their price is low, g) dimers, trimers, up to polymers compounds show high electronic conjugation or show charge transference that makes them colored compounds, stable at room temperature and atmospheric pressure, h) The products obtained through the process of the current invention, dimers, trimers, oligomers up to polymers are produced which are stable with outstanding properties that make them useful in the fields of electronics, optical and as inhibitors in polymerization and as antioxidants.

SUMMARY OF THE INVENTION

The present invention is directed to ethenediol products and a process to obtain ethenediols from pyridine derivative compounds. The various aspects of the invention are attained by providing a process for obtaining dimers, trimers, up to polymers from pyridinmethanol derived compounds, characterized in that it comprises reacting a compound of general formula (I) according to the following reaction:

wherein R stands for H or —CH₃, in a coupling reaction, at a temperature of approximately 120 to 160° C., the reaction is catalyzed by temperature, the reaction time is approximately from 5 to 24 hrs., atmospheric pressure is used, the products are obtained by precipitation with a 2N NaOH solution, 2N HCl solution or H₂O, and correspond to a general formula (III), having an appearance of yellow-brown powders.

BRIEF DESCRIPTION OF THE DRAWINGS

The following is a brief description of the drawings, in which:

FIG. 1 is an IR spectrum of 1,2-di(2-pyridyl)ethene-1,2-diol;

FIG. 2 is an NMR spectrum of 1,2-di(2-pyridyl)ethene-1,2-diol;

FIG. 3 is an IR spectrum of 1,2-bis(6-methylpyridin-2-yl)ethene-1,2-diol; and

FIG. 4 is an electronic impact spectrum of 1,2-bis(6-methylpyridin-2-yl)ethene-1,2-diol.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

As far as the knowledge of the applicant goes, there is no precedent about polymeric structures that contain in their structure parts such as —C(OH)═C(OH)—, —CO—CO— or —COH—CO— and that are produced from pyridinealcohols, as well as some known to date chemical process that discloses the dimerization or coupling of alcohols.

According to the current invention pyridinemethanol derivatives are used for the first time to react them to form compounds with repetitive structural entities of 1,2-(2-pyridyl)-etheno-1,2-diols.

The Percino-Chapela process of the current invention consists of a one step mass reaction. The reactions contemplated as of general character reactions that represent this process are shown in Reactions 6, 7 and 8. The process consists of the following stages: a) pyridinemethanol derivatives with general formula (I), wherein R represents H or CH₃, are made to react to get a product of the general formula (III), wherein R is H or CH₃; pyridinemethanol derivatives with a general formula (II), wherein R is CH₃ or —CH₂—OH, are made to react to get a product of the general formula (IV), wherein R is H or CH₃ and R′ is H or —COH═COH—C₅H₅N, the reaction is carried out under reflux and without solvents for an approximate time between 5 and 24 hours at temperatures ranging from approximately 120 to 160° C., at atmospheric pressure; b) afterward the reaction mixture is precipitated by adding 1-3 N HCl solution, 1-3 N NaOH solution or water, to produce mainly powder of different colors.

Sometimes it is necessary to add a catalyst when the reaction is very slow or when the product yield is low after a long reaction time. A catalyst such as pyridine, triethylamine or similar base is made to react along with the reactant in a molar relationship between 0.5-1 relative to the reactant to react. The reaction is not an instantaneous one, starting from approximately 1:30 hrs. color changes start, mainly from yellow, red-orange, brown and darker. The products are brown and orange powders, soluble in cyclohexane, methanol, and DMSO, with melting point within the range of 100 to 250° C. Which may indicate a high electronic conjugation in the structure.

When in reaction 8 the general compound (II) has —CH₂OH as equivalent for R and this is the only reactant in the reaction, the result are products with general formula (V) the meaning of R₁ being —OH or ═O and R₂ being —OH or ═O, R₁ and R₂ being the same or different, when R₁ or R₂ is ═O the α bond is a single bond.

In order to illustrate the process of the current invention, the following examples of the uses of the invention are described below.

EXAMPLES Example 1

The current example refers to general reaction 6; it is carried out as a coupling reaction using as starting chemicalinitial 2-pyridinmethanol recently distilled, the reaction is catalyzed with temperature, the values of which are approximately 153 to 155° C. It is carried out under atmospheric pressure, for approximately 24 hours, pyridine is added as a catalyst in a molar ratio 1:1. The products corresponding to general formula (III) are obtained through precipitation with a solution of 2N NaOH, 2N HCl or H₂O, they have got a yellow-brown powder appearance, which were characterized through the analytical techniques known as IR Infrared, Nuclear Magnetic Resonance NMR′H and mass spectrometry, in FIG. 1 the IR spectrum is shown, and in FIG. 2 that of the NMR.

The evidence through IR which indicated the presence of the 1,2-di(2-pyridyl)-1,2-ethenediol in Example 1 (FIG. 1) was the band at 3448 to 3421 cm⁻¹ assigned to the νO—H vibration, the band at 1180 cm⁻¹ assigned to the νC—O vibration of alcohol, and the band at 1590 cm⁻¹ assigned to the νC═N vibration of the pyridinic ring.

In FIG. 2, the NMR proton spectrum for the 1,2-di(2-pyridyl) 1,2-ethenediol. The molecule is symmetrical and therefore the signals that indicated its formation were a wide signal at 12.923 ppm assigned to the OH proton (a) with an integration of 2H, the multiplet between 8.479-8.453 ppm corresponds to the two protons in position 6 of the pyridinic ring (b), the multiplet between 7.930-7.808 ppm can be assigned to four protons of both rings; two protons one in position 4 and two in position 3 of the ring (c). Lastly, the multiple signals between 7.21-7.166 ppm was assigned to the two protons in position 5 of the pryridinic ring (d)

The evidence from IR FIG. 3, which indicated the presence of 1,2-bis(6-methylpyridin-2-yl)ethene-1,2-diol was the band at 1226 cm⁻¹ assigned to the νC—O vibration of alcohol and the band at 1180 cm⁻¹ owing to the deformation vibration of the O—H. The bands at 1590 and 1569 cm⁻¹ assigned to the νC═N and C═C vibration of the pryridinic ring. The band a 3448-3421 cm⁻¹ assigned to the νO—H vibration. The mass spectrum FIG. 4, gave the molecular ion 242 m/z (M+), which corresponds to the theoretical molecular weight of 242 g/Mol for the 1,2-bis[2-(6-methylpyridin-1-yl)ethene-1,2-diol].

The products obtained when the meaning of R is hydrogen are: 1,2-di(pyridin-2-yl)ethene-1,2-diol and 1,2-di(pyridin-4-yl)ethene-1,2-diol.

Example 2

The Example refers to general reaction 7; to obtain oligomers, the molar relation used is 1:1 of 6-methyl-2-pyridinemethanol to 2-pyridinemethanol, the reaction is carried out at a temperature of approximately 140° C., at atmospheric pressure, for approximately 24 hours. The product is obtained when the solution is precipitated with 2 N NaOH, the product obtained corresponds to the general formula (IV), and it has a molecular weight in the interval of 228 g/mol. The product is an orange or brown powder, soluble in CHCl₃, C₆H₁₂, cyclohexane and THF, with a melting point of 128-133° C.

The product preferably obtained is [1-(6-methylpyridin-2-yl)-2-(pyridin-2′-yl)]ethene-1,2-diol.

Example 3

Similar to Example 2, a reaction is carried out where the reactants molar ratio is 1:2 of 2,6-pyridinedimethanol with 2-pyridinemethanol. The reaction conditions used were: a temperature of approximately 140° C., at atmospheric pressure for about 24 hours, the resulting product corresponds to general formula (IV), and has a molecular weight of 243 or 333 g/mol depending on whether it is of two or three rings with terminal groups —CH₂OH. The products are dark brown powders soluble in CH₃OH and DMSO, with melting point of 200-250° C.

The product preferably obtained is 2,6-di[(pyridin-2′-yl)ethene-1,2-diol]-COH═COH—NC₅H₅

Example 4

This is similar to Examples 1 and 2, the example specifically refers to general reaction 8, which is carried out using pyrindinedimethanols to obtain polymers such as: poly[2-hydroxy-(1,2-di(pyridin-2-yl)ethane-1-one], poly[1,2-di(pyridin-2-yl)ethane-1,2-dione] and poly[1,2-di(pyridin-2-yl)ethene-1,2-diol] with grade of polymerization n in an interval of 10-30 monomeric units, these are obtained as a brown soluble powder in DMSO with melting point between 161-164° C., by precipitation with 2N HCl solution, after a reaction time of 24 hours, reaction temperature of 140° C. at atmospheric pressure. The molecular weight is approximately between 2182-6422 g/mol.

The products obtained with ethenediol parts can be applied as antioxidants due to their capacity as free radical inhibitors. 

What is claimed is:
 1. Process for obtaining dimers, trimers, up to polymers from pyridinmethanol derived compounds, characterized in that it comprises reacting a compound of general formula (I) according to the following reaction:

wherein R stands for H or —CH₃, in a coupling reaction, at a temperature of approximately 120 to 160° C., the reaction is catalyzed by temperature, the reaction time is approximately from 5 to 24 hrs., atmospheric pressure is used, the products are obtained by precipitation with a 2N NaOH solution, 2N HCl solution or H₂O, and correspond to a general formula (III), having an appearance of yellow-brown powders.
 2. The process for producing dimers, trimers up to polymers from pyridinemethanol derived compound according to claim 1, characterized in that a general formula of compound (II) is reacted according to the following reaction:

wherein R stands for H, CH₃ or —CH₂—OH, the reaction temperature is of approximately 120 to 160° C., the reaction time is approximately 5 to 24 hrs. the resultant products correspond to the general formula (IV), wherein R means H or —CH₃ and R′ means H or —COH═COH—C₅H₅N, with a molecular weight of approximately 213 to 333 g/mol.
 3. The process for producing dimers, trimers up to polymers from pyridinemethanol derivative compounds according to claim 2, characterized in that the production of oligomers, the molar relationship used is 1:1 of 6-methyl-2-pyridinmethanol with 2-pyridinmethanol, the reaction is carried out at a temperature of approximately 120 to 160° C., at atmospheric pressure, for a 5 to 24 hrs lapse, the product is produced by precipitation with a 2N NaOH solution and has a molecular weight in the interval of 228 g/mol, the product is preferably the [1-(6-methylpyridin-2-yl)-2-(pyridin-2′-yl)]ethene-1,2-diol, which is an orange or brown powder soluble in CHCl₃, C₆H₁₂, cyclohexane and THF, with a melting point of 128-133° C.
 4. The process for producing dimers, trimers up to polymers from pyridinmethanol derivative compounds according to claim 2, characterized in that the molar ratio of the reagents is of 1:2 of 2,6-pyridinedimethanol to 2-pyridinemethanol, the reaction temperature is of approximately 120 to 160° C., the reaction time is of approximately 5 to 24 hrs, the resultant product is preferably 2,6-di[(pyridin-2′-il)ethene-1,2-diol]-COH═COH—NC₅H₅ with a molecular weight of approximately 213 to 333 g/mol.
 5. The process for producing dimers, trimers up to polymers from pyridinmethanol derivative compounds according to claim 1, characterized for it is carried out according to the following reaction:

wherein R₁ stands for —OH or ═O and R₂ stands for —OH or ═O, wherein R₁ and R₂ are either the same or different, when R₁ or R₂ is ═O, the α bond is a single bond, the resultant products are a brown powder soluble in DMSO with melting point between 161-164° C. produced by precipitation with an 2N HCl solution, after a 24 hr reaction time, reaction temperature of 140° C. at atmospheric pressure, the compounds are produced with a polymerization grade n in a 10-30 monomeric units interval with a molecular weight of approximately 2182-6422 g/mol.
 6. The process for producing dimers, trimers up to polymers from pyridinemethanol derivative compounds according to claim 5, characterized by the fact that the resultant products of this reaction are preferably: Poly[2-hydroxy-(1,2-di(pyridin-2-yl)ethane-1-one]; poly[1,2-di(pyridin-2-yl)ethane-1,2-dione] and poly[1,2-di(pyridin-2-yl)ethene-1,2-diol] with a polymerization grade n in a 10-30 monomeric units interval.
 7. The process for producing dimers, trimers up to polymers from pyridinmethanol derivative compounds according to claim 1, characterized in that a catalyst such as pyridine, triethylamine or similar base, reacts with the reactant in a molar relationship between 0.5-1 relative to the reactant used for the reaction.
 8. The products resultant of the process of claim 1, characterized for being represented by the following formula:

wherein R stands for H or —CH₃, being either equal or different.
 9. The products resultant according to claim 8, characterized in that it is represented by formula (III) and that correspond preferably to the following: 1,2-di(pyridin-2-yl)ethene-1,2-diol; 1-2di(pyridin-4-yl)ethene-1,2-diol; 1,2bis(methylpiridin-2-yl)ethene-1,2-diol; 1,2-bis(4-methylpyridin-2-yl)ethene-1,2-diol; 1,2-bis(6-methylpyridin-2-yl)ethene-1,2-diol.
 10. The products resultant from the process of claim 1, characterized in that they are represented by formula (IV),

wherein R stands for H, —CH₃ and —CH₂OH, R′ stands for H or —COH═COH—C₅H₅N, with a molecular weight of approximately 213 to 333 g/mol.
 11. The products according to claim 10, characterized for they are represented by formula (IV) and correspond preferably to the following [1-(6-methylpiridin-2-yl)-2-(piridin-2′-yl)]ethene-1,2-diol and 2,6-di[(pyridin-2′-yl)ethene-1,2-diol]_COH═COH—NC₅H₅ with a molecular weight of approximately 213 to 333 g/mol.
 12. The products resultant from the process of claim 1, characterized for they are represented by formula (V)

wherein R₁ stands for —OH or ═O and R₂ for —OH or ═O, being R₁ and R₂ equal or different, when R₁ or R₂ is ═O the α bond is a single bond, with a polymerization grade n in an interval of 10-30 monomeric units.
 13. The products according to claim 12, characterized for they are represented by the general formula (V) and are preferably: poly[2-hydroxy-(1,2-di(pyridin-2-yl)ethane-1-one], poly[1,2-di(pyridin-2-yl)ethane-1,2-dione] and poly[1,2-di(pyridin-2-yl)ethene-1,2-diol] with a polymerization grade n in an interval of 10-30 monomeric units.
 14. The process of claim 1, wherein the reaction temperature is from 153° C. to 155° C. and the reaction time is approximately 24 hours.
 15. The process of claim 2, wherein the reaction temperature is approximately 140° C. and the reaction time is approximately 24 hours.
 16. The process of claim 3, wherein the reaction temperature is approximately 140° C. and the reaction time is approximately 24 hours.
 17. The process of claim 4, wherein the reaction temperature is approximately 140° C. and the reaction time is approximately 24 hours. 